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利用各种颜色的细胞器靶向荧光探针混合物对铁死亡过程中不稳定的 Fe(ii)进行细胞器特异性分析。

Organelle-specific analysis of labile Fe(ii) during ferroptosis by using a cocktail of various colour organelle-targeted fluorescent probes.

机构信息

Laboratory of Pharmaceutical and Medicinal Chemistry, Gifu Pharmaceutical University, Japan.

出版信息

Metallomics. 2019 Jan 23;11(1):111-117. doi: 10.1039/c8mt00212f.

Abstract

Ferroptosis is an emerging type of cell death mode that is dependent on iron. Unfortunately, the detailed analysis of the function of organelle labile Fe(ii) in oxidative damage and lethality of the cells has not been demonstrated so far, mainly due to the lack of efficient methods to visualize labile Fe(ii) at the targeted organelles. We have recently reported a series of Fe(ii)-selective fluorescent probes, i.e., Ac-MtFluNox, Lyso-RhoNox, and ER-SiRhoNox, which can detect Fe(ii) specifically in the mitochondria, lysosomes, and endoplasmic reticulum (ER), respectively. These probes demonstrate similar reaction rates and off/on contrasts with various colours and intracellular distributions, enabling simultaneous multi-colour imaging that allows the monitoring of labile Fe(ii) levels at each targeted organelle. In this paper, by using a cocktail of these probes, we successfully visualised the aberrant elevation of labile Fe(ii) in the lysosomes and ER prior to HT1080 cell death induced by erastin, which is an inducer of ferroptosis.

摘要

铁死亡是一种依赖于铁的新型细胞死亡模式。不幸的是,目前还没有对细胞器不稳定的 Fe(ii) 在细胞氧化损伤和致死性中的作用进行详细分析,主要是因为缺乏有效的方法来在靶向细胞器中可视化不稳定的 Fe(ii)。我们最近报道了一系列 Fe(ii) 选择性荧光探针,即 Ac-MtFluNox、Lyso-RhoNox 和 ER-SiRhoNox,它们分别可以在线粒体、溶酶体和内质网(ER)中特异性检测 Fe(ii)。这些探针具有相似的反应速率和开/关对比度,颜色和细胞内分布也相似,能够进行同时的多色成像,从而可以监测每个靶向细胞器中不稳定的 Fe(ii)水平。在本文中,通过使用这些探针的混合物,我们成功地观察到在 erastin(诱导铁死亡的一种试剂)诱导 HT1080 细胞死亡之前,溶酶体和 ER 中不稳定的 Fe(ii)异常升高。

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